69541-62-4 Usage
Uses
Used in Pharmaceutical Development:
BOC-D-TYR(2,6-DI-CL-BZL)-OH is used as a building block in the synthesis of peptide chains for the development of peptide-based pharmaceuticals. Its protective groups facilitate the controlled assembly of complex peptide structures, which are vital for the creation of new drugs with specific therapeutic properties.
Used in Research and Development:
In the research and development industry, BOC-D-TYR(2,6-DI-CL-BZL)-OH is used as a research tool to study the structure and function of proteins and peptides. Understanding these fundamental aspects is crucial for advancing knowledge in biochemistry and for the discovery of new therapeutic agents.
Used in Biochemistry Education:
BOC-D-TYR(2,6-DI-CL-BZL)-OH can also be utilized in educational settings to teach students about the synthesis of peptides and the importance of protective groups in organic chemistry and biochemistry. This helps in fostering a deeper understanding of the principles underlying drug development and protein research.
Check Digit Verification of cas no
The CAS Registry Mumber 69541-62-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,5,4 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69541-62:
(7*6)+(6*9)+(5*5)+(4*4)+(3*1)+(2*6)+(1*2)=154
154 % 10 = 4
So 69541-62-4 is a valid CAS Registry Number.
69541-62-4Relevant academic research and scientific papers
Synthesis and biological activity of N-substituted aminocarbonyl-1,3- dioxolanes as VLA-4 antagonists
Rehman, Abdul,Soni, Ajay,Naik, Keshav,Nair, Sreeji,Palle, Venkata P.,Dastidar, Sunanda,Ray, Abhijit,Alam,Salman, Mohammad,Cliffe, Ian A.,Sattigeri, Viswajanani
scheme or table, p. 5514 - 5520 (2011/01/12)
A novel set of compounds with a 1,3-dioxolane ring which acts as a proline bioisostere have been successfully designed as VLA-4 receptor antagonists. Compounds (18e), (28j), and (35g) were shown to have high receptor affinities.
A simple method for the alkaline hydrolysis of esters
Theodorou, Vassiliki,Skobridis, Konstantinos,Tzakos, Andreas G.,Ragoussis, Valentine
, p. 8230 - 8233 (2008/03/14)
A very mild and rapid procedure for the efficient alkaline hydrolysis of esters in non-aqueous conditions has been developed, by the use of dichloromethane/methanol (9:1) as solvent. This method conveniently provides both carboxylic acids and alcohols from the corresponding esters and sodium hydroxide in a few minutes at room temperature. A plausible reaction mechanism is proposed.
